{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Araszczuk AM"],"funding":["Ministero dell&apos;Universit? e della Ricerca","Universit? degli Studi di Salerno"],"pagination":["7752-7756"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9623583"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["24(42)"],"pubmed_abstract":["Head-to-tail cyclization of linear oligoamides containing 4-benzylaminomethyl-1<i>H</i>-1,2,3-triazol-1-yl acetic acid monomers afforded a novel class of \"extended macrocyclic peptoids\". The identification of the conformation in solution for a cyclodimer and the X-ray crystal structure of a cyclic tetraamide are reported."],"journal":["Organic letters"],"pubmed_title":["Macrocyclic Triazolopeptoids: A Promising Class of Extended Cyclic Peptoids."],"pmcid":["PMC9623583"],"funding_grant_id":["2020AEX4TA"],"pubmed_authors":["Della Sala G","D'Amato A","Araszczuk AM","Pierri G","Tedesco C","Schettini R","Costabile C","Izzo I","De Riccardis F"],"additional_accession":[]},"is_claimable":false,"name":"Macrocyclic Triazolopeptoids: A Promising Class of Extended Cyclic Peptoids.","description":"Head-to-tail cyclization of linear oligoamides containing 4-benzylaminomethyl-1<i>H</i>-1,2,3-triazol-1-yl acetic acid monomers afforded a novel class of \"extended macrocyclic peptoids\". The identification of the conformation in solution for a cyclodimer and the X-ray crystal structure of a cyclic tetraamide are reported.","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Oct","modification":"2025-04-18T22:51:54.583Z","creation":"2025-04-07T10:36:07.291Z"},"accession":"S-EPMC9623583","cross_references":{"pubmed":["36223077"],"doi":["10.1021/acs.orglett.2c03062"]}}